[go: up one dir, main page]

BR9307648A - Pyrazolopyrimidines as crf antagonists - Google Patents

Pyrazolopyrimidines as crf antagonists

Info

Publication number
BR9307648A
BR9307648A BR9307648A BR9307648A BR9307648A BR 9307648 A BR9307648 A BR 9307648A BR 9307648 A BR9307648 A BR 9307648A BR 9307648 A BR9307648 A BR 9307648A BR 9307648 A BR9307648 A BR 9307648A
Authority
BR
Brazil
Prior art keywords
pyrazolopyrimidines
crf antagonists
scr1r2r11
ocr1r2r11
nhnr1r2
Prior art date
Application number
BR9307648A
Other languages
Portuguese (pt)
Inventor
Yuhpyng Liang Chen
Original Assignee
Pfizer
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of BR9307648A publication Critical patent/BR9307648A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/26—Psychostimulants, e.g. nicotine, cocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Immunology (AREA)
  • Psychiatry (AREA)
  • Virology (AREA)
  • Pulmonology (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Transplantation (AREA)
  • Oncology (AREA)
  • Rheumatology (AREA)
  • Communicable Diseases (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

A compound of the formula:and the pharmaceutically acceptable acid addition salts thereof, whereinA is NR1R2, CR1R2R11, or C(=CR1R12)R2, NHCR1R2R11, OCR1R2R11, SCR1R2R11, NHNR1R2, CR2R11NHR1, CR2R11OR1, CR2R11SR1 or C(O)R2;wherein the rest of the variables are herein below defined, used for inflammatory disorders.
BR9307648A 1992-12-17 1993-11-26 Pyrazolopyrimidines as crf antagonists BR9307648A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US99222992A 1992-12-17 1992-12-17
PCT/US1993/011333 WO1994013677A1 (en) 1992-12-17 1993-11-26 Pyrazolopyrimidines as crf antagonists

Publications (1)

Publication Number Publication Date
BR9307648A true BR9307648A (en) 1999-05-25

Family

ID=25538069

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9307648A BR9307648A (en) 1992-12-17 1993-11-26 Pyrazolopyrimidines as crf antagonists

Country Status (27)

Country Link
US (1) US6218397B1 (en)
EP (1) EP0674642B1 (en)
JP (1) JP2862375B2 (en)
KR (2) KR0167395B1 (en)
CN (1) CN1034175C (en)
AT (1) ATE195738T1 (en)
AU (1) AU680226B2 (en)
BR (1) BR9307648A (en)
CA (1) CA2150709C (en)
CZ (1) CZ287319B6 (en)
DE (1) DE69329296T2 (en)
DK (1) DK0674642T3 (en)
EG (1) EG20273A (en)
ES (1) ES2150482T3 (en)
FI (1) FI105920B (en)
GR (1) GR3034507T3 (en)
HU (1) HU221507B (en)
IL (1) IL107944A (en)
MY (1) MY115300A (en)
NO (1) NO305437B1 (en)
NZ (1) NZ259114A (en)
PL (1) PL177028B1 (en)
PT (1) PT674642E (en)
RU (1) RU2124016C1 (en)
TW (2) TW444018B (en)
WO (1) WO1994013677A1 (en)
ZA (1) ZA939405B (en)

Families Citing this family (169)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW444018B (en) * 1992-12-17 2001-07-01 Pfizer Pyrazolopyrimidines
PL313973A1 (en) 1993-10-12 1996-08-05 Du Pont Merck Pharma 1 n-alkyl-n-arylopyrimidin amines and their derivatives
US5654307A (en) * 1994-01-25 1997-08-05 Warner-Lambert Company Bicyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family
IL112249A (en) 1994-01-25 2001-11-25 Warner Lambert Co Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
IL112248A0 (en) 1994-01-25 1995-03-30 Warner Lambert Co Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
AU1884595A (en) * 1994-04-29 1995-11-29 Pfizer Inc. Novel acyclic and cyclic amides as neurotransmitter release enhancers
FR2719587B1 (en) * 1994-05-03 1996-07-12 Roussel Uclaf New erythromycin derivatives, their preparation process and their use as drugs.
TW530047B (en) * 1994-06-08 2003-05-01 Pfizer Corticotropin releasing factor antagonists
US5646152A (en) * 1994-06-15 1997-07-08 Pfizer Inc. Methods of administering CRF antagonists
CN1056611C (en) * 1994-06-16 2000-09-20 美国辉瑞有限公司 Pyrazolo and pyrrolopyridines
EP0729758A3 (en) * 1995-03-02 1997-10-29 Pfizer Pyrazolopyrimidines and pyrrolopyrimidines to treat neuronal disorders and other diseases
US5593997A (en) * 1995-05-23 1997-01-14 Pfizer Inc. 4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors
US7125880B1 (en) 1995-06-06 2006-10-24 Pfizer Inc. Corticotropin releasing factor antagonists
US6403599B1 (en) 1995-11-08 2002-06-11 Pfizer Inc Corticotropin releasing factor antagonists
US5747495A (en) * 1995-08-22 1998-05-05 Hiroshi Maeda Method for treating hypertension using pyrazolopyrimidine derivatives
US6992188B1 (en) 1995-12-08 2006-01-31 Pfizer, Inc. Substituted heterocyclic derivatives
ATE243697T1 (en) * 1995-12-08 2003-07-15 Pfizer SUBSTITUTED HETEROCYCLIC DERIVATIVES AS CRF ANTAGONISTS
EP0882051B1 (en) 1996-02-07 2001-11-07 Janssen Pharmaceutica N.V. Thiophenopyrimidines
CN1090189C (en) * 1996-02-07 2002-09-04 詹森药业有限公司 Pyrazolopyrimidines
US6664261B2 (en) 1996-02-07 2003-12-16 Neurocrine Biosciences, Inc. Pyrazolopyrimidines as CRF receptor antagonists
US6051578A (en) * 1996-02-12 2000-04-18 Pfizer Inc. Pyrazolopyrimidines for treatment of CNS disorders
AU725254B2 (en) * 1996-03-26 2000-10-12 Du Pont Pharmaceuticals Company Aryloxy- and arylthio- fused pyridines and pyrimidines and derivatives
US6107300A (en) * 1996-03-27 2000-08-22 Dupont Pharmaceuticals Arylamino fused pyrimidines
CN1066448C (en) * 1996-06-06 2001-05-30 株式会社大塚制药工场 Amide derivatives
US6313124B1 (en) 1997-07-23 2001-11-06 Dupont Pharmaceuticals Company Tetrazine bicyclic compounds
US6124289A (en) * 1996-07-24 2000-09-26 Dupont Pharmaceuticals Co. Azolo triazines and pyrimidines
US6191131B1 (en) 1997-07-23 2001-02-20 Dupont Pharmaceuticals Company Azolo triazines and pyrimidines
US7094782B1 (en) 1996-07-24 2006-08-22 Bristol-Myers Squibb Company Azolo triazines and pyrimidines
US6060478A (en) * 1996-07-24 2000-05-09 Dupont Pharmaceuticals Azolo triazines and pyrimidines
KR20000029843A (en) * 1996-08-06 2000-05-25 디. 제이. 우드;스피겔 알렌 제이 Substituted pyrido- or pyrimido-containing 6,6- or 6,7-bicyclic derivatives
US5861398A (en) * 1996-08-26 1999-01-19 Alanex Corporation Benzoperimidine-carboxylic acids and derivatives thereof
TW477787B (en) * 1996-08-27 2002-03-01 Pfizer Pyrido six-membered nitrogen-containing cyclic ring derivatives having corticotropin releasing factor antagonist activity and pharmaceutical composition containing same
ATE213495T1 (en) * 1996-09-16 2002-03-15 Du Pont Pharm Co SURGICAL IMPLANT CONTAINING AN ABSORBABLE RADIO-OPACQUE MARKER AND METHOD FOR LOCKING THE SAME INTO A BODY
US5723608A (en) * 1996-12-31 1998-03-03 Neurogen Corporation 3-aryl substituted pyrazolo 4,3-d!pyrimidine derivatives; corticotropin-releasing factor receptor (CRF1) specific ligands
EP0970082A2 (en) * 1997-02-18 2000-01-12 Neurocrine Biosciences, Inc. Biazacyclic crf antagonists
SE9701398D0 (en) * 1997-04-15 1997-04-15 Astra Pharma Prod Novel compounds
US6245769B1 (en) * 1997-09-02 2001-06-12 Dupont Pharmaceuticals Company Heterocyclyl-substituted ring-fused pyridines and pyrimidines as corticotropin releasing hormone(CRH) antagonists, useful for treating CNS and stress-related disorders
US6613777B1 (en) 1998-03-06 2003-09-02 Chen Chen CRF antagonistic pyrazolo[4,3-b]pyridines
US6472402B1 (en) 1998-04-02 2002-10-29 Neurogen Corporation Aminoalkyl substituted 5,6,7,8-Tetrahydro-9H-Pyridino [2,3-B]indole derivatives
CA2326319A1 (en) 1998-04-02 1999-10-14 Neurogen Corporation Aminoalkyl substituted 5,6,7,8-tetrahydro-9h pyrimidino[2,3-b]indole and 5,6,7,8-tetrahydro-9h-pyrimidino[4,5-b]indole derivatives: crf1 specific ligands
US6984667B2 (en) * 1998-04-08 2006-01-10 Theta Biomedical Consulting And Development Co. Synergistic proteoglycan compositions for inflammatory conditions
US6531477B1 (en) 1998-10-13 2003-03-11 Dupont Pharmaceuticals Company 6-substituted pyrazolo [3,4-d] pyrimidin-4-ones useful as cyclin dependent kinase inhibitors
US6559152B2 (en) * 1998-10-13 2003-05-06 Dupont Pharmaceuticals Company 6-substituted pyrazolo[3,4-d]pyrimidin-4-ones useful as cyclin dependent kinase inhibitors
US6531475B1 (en) 1998-11-12 2003-03-11 Neurocrine Biosciences, Inc. CRF receptor antagonists and methods relating thereto
PT1129096E (en) * 1998-11-12 2003-09-30 Neurocrine Biosciences Inc CRF RECEPTOR ANTAGONISTS AND METHODS OF TREATMENT RELATED TO THEM
ATE225349T1 (en) 1998-11-12 2002-10-15 Neurocrine Biosciences Inc CRF RECEPTOR ANTAGONISTS AND RELATED METHODS
EP1040831A3 (en) 1999-04-02 2003-05-02 Pfizer Products Inc. Use of corticotropin releasing factor (CRF) antagonists to prevent sudden death
US6387894B1 (en) 1999-06-11 2002-05-14 Pfizer Inc. Use of CRF antagonists and renin-angiotensin system inhibitors
US6409988B1 (en) 1999-07-01 2002-06-25 3-Dimensional Pharmaceuticals, Inc. Radiolabeled 1-aryl pyrazoles, the synthesis thereof and the use thereof as pest GABA receptor ligands
US6506784B1 (en) 1999-07-01 2003-01-14 3-Dimensional Pharmaceuticals, Inc. Use of 1,3-substituted pyrazol-5-yl sulfonates as pesticides
WO2001007413A1 (en) 1999-07-22 2001-02-01 3-Dimensional Pharmaceuticals, Inc. 1-aryl-3-thioalkyl pyrazoles, the synthesis thereof and the use thereof as insecticides
US6432989B1 (en) 1999-08-27 2002-08-13 Pfizer Inc Use of CRF antagonists to treat circadian rhythm disorders
AU7738000A (en) 1999-09-30 2001-04-30 Neurogen Corporation Certain alkylene diamine-substituted heterocycles
WO2001025241A2 (en) 1999-10-06 2001-04-12 3-Dimensional Pharmaceuticals, Inc. Fused 1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazoles, the synthesis thereof and the use thereof as pesticides
IL139197A0 (en) 1999-10-29 2001-11-25 Pfizer Prod Inc Use of corticotropin releasing factor antagonists and related compositions
US6525067B1 (en) * 1999-11-23 2003-02-25 Pfizer Inc Substituted heterocyclic derivatives
TWI271406B (en) 1999-12-13 2007-01-21 Eisai Co Ltd Tricyclic condensed heterocyclic compounds, preparation method of the same and pharmaceuticals comprising the same
AU2001232271A1 (en) * 2000-02-14 2001-08-20 Japan Tobacco Inc. Preventives/remedies for postoperative stress
US20060223824A1 (en) 2000-11-28 2006-10-05 Wyeth Serotonergic agents
US20060287335A1 (en) 2000-11-28 2006-12-21 Wyeth Serotonergic agents for treating sexual dysfunction
GB0100621D0 (en) 2001-01-10 2001-02-21 Vernalis Res Ltd Chemical compounds VI
TWI312347B (en) 2001-02-08 2009-07-21 Eisai R&D Man Co Ltd Bicyclic nitrogen-containing condensed ring compounds
US7605175B2 (en) 2001-03-02 2009-10-20 Gpc Biotech Ag Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
RS50863B (en) 2001-03-13 2010-08-31 Bristol-Myers Squibb Pharma Company 4- (2-BUTYLAMINO) -2,7-DIMETHYL-8- (2-METHYL-6-METHOXYPYRID-3-YL) PYRAZOLO / 1,5A / -1,3,5-TRIAZINE, ITS ENANTIOMERS AND PHARMACEUTICAL ACCEPTABLE SALTS AS A RECEPTOR LIGANDS FOR A FACTOR THAT CREATES CORTICOTROPINE
PL214231B1 (en) 2001-04-27 2013-07-31 Eisai R & D Man Co Pyrazolo[1,5-a]pyridines and medicines containing the same
IL144900A (en) 2001-08-14 2013-12-31 Neurim Pharma 1991 Melatonin and medicaments comprising it for use in treating primary insomnia and in the manufacture of such medicaments
US6638981B2 (en) 2001-08-17 2003-10-28 Epicept Corporation Topical compositions and methods for treating pain
DE10219435A1 (en) * 2002-05-02 2003-11-13 Bayer Cropscience Ag Substituted pyrazolo-pyrimidin-4-ones
TW200400034A (en) 2002-05-20 2004-01-01 Bristol Myers Squibb Co Pyrazolo-pyrimidine aniline compounds useful as kinase inhibitors
TWI259083B (en) * 2002-05-24 2006-08-01 Nat Health Research Institutes Anti-enterovirus compounds
KR100468352B1 (en) * 2002-09-24 2005-01-27 한국과학기술연구원 New pyrazolopyrimidine derivatives, process for their preparation and pharmaceutical composition comprising the same
TWI283679B (en) 2002-10-22 2007-07-11 Eisai Co Ltd 7-phenylpyrazolopyridine compounds
US7176216B2 (en) 2002-10-22 2007-02-13 Eisai Co., Ltd. 7-phenylpyrazolopyridine compounds
WO2004054566A1 (en) 2002-12-13 2004-07-01 Warner-Lambert Company Llc Pregabalin derivatives for the treatment of fibromyalgia and other disorders
CN102558155A (en) 2003-01-14 2012-07-11 阿伦纳药品公司 Aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of diseases related thereto, such as diabetes and hyperglycemia
US7786112B2 (en) 2003-04-07 2010-08-31 Agennix Usa Inc. Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
US7834014B2 (en) 2003-04-09 2010-11-16 Biogen Idec Ma Inc. A2a adenosine receptor antagonists
WO2004092177A1 (en) 2003-04-09 2004-10-28 Biogen Idec Ma Inc. Triazolopyrazines and methods of making and using the same
WO2004092170A2 (en) 2003-04-09 2004-10-28 Biogen Idec Ma Inc. Triazolotriazines and pyrazolotriazines useful as a2a adenosine receptor antagon ists
NZ544301A (en) * 2003-06-25 2008-08-29 Ono Pharmaceutical Co Methanesulfonic acid salt of pyrazolopyrimidine compound, crystal thereof, and process for producing the same
AR045047A1 (en) 2003-07-11 2005-10-12 Arena Pharm Inc ARILO AND HETEROARILO DERIVATIVES TRISUSTITUIDOS AS MODULATORS OF METABOLISM AND PROFILAXIS AND TREATMENT OF DISORDERS RELATED TO THEMSELVES
AU2004257267B2 (en) * 2003-07-14 2009-12-03 Arena Pharmaceuticals,Inc Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto
US7160888B2 (en) 2003-08-22 2007-01-09 Warner Lambert Company Llc [1,8]naphthyridin-2-ones and related compounds for the treatment of schizophrenia
AU2004274403A1 (en) * 2003-09-03 2005-03-31 Aventis Pharmaceuticals Inc. 5-aryl-Pyrazolo(4,3-d)pyrimidines, pyridines, and pyrazines and related compounds
GB0326168D0 (en) * 2003-11-10 2003-12-17 Arrow Therapeutics Ltd Chemical compounds
GB0327319D0 (en) * 2003-11-24 2003-12-24 Pfizer Ltd Novel pharmaceuticals
US7572799B2 (en) 2003-11-24 2009-08-11 Pfizer Inc Pyrazolo[4,3-d]pyrimidines as Phosphodiesterase Inhibitors
EA013117B1 (en) 2003-12-23 2010-02-26 ДжиПиСи БАЙОТЕК, ИНК. Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
CA2556450C (en) * 2004-02-17 2013-08-06 Transoral Pharmaceuticals, Inc. Compositions for delivering hypnotic agents across the oral mucosa and methods of use thereof
CN100548281C (en) * 2004-02-17 2009-10-14 创塞伯特制药公司 Compositions for delivering hypnotic agents across the oral mucosa and uses thereof
KR20140104986A (en) * 2004-02-17 2014-08-29 트랜스셉트 파마슈티칼스, 인코포레이티드 Compositions for delivering hypnotic agents across the oral mucosa and methods of use thereof
US20080287405A1 (en) * 2004-05-14 2008-11-20 Thannickal Victor J Compositions and Methods Relating to Protein Kinase Inhibitors
EP1831225A2 (en) 2004-11-19 2007-09-12 The Regents of the University of California Anti-inflammatory pyrazolopyrimidines
AU2006239920A1 (en) * 2005-04-22 2006-11-02 Wyeth Dihydrobenzofuran derivatives and uses thereof
CN101203216A (en) * 2005-04-22 2008-06-18 惠氏公司 Dihydrobenzofuran derivatives and uses thereof
MX2007013179A (en) * 2005-04-22 2008-01-16 Wyeth Corp Crystal forms of {[(2r)-7-(2,6-dichlorophenyl)-5-fluoro-2,3- dihydro-1-benzofuran-2-yl]methyl}amine hydrochloride.
CN101203218A (en) * 2005-04-22 2008-06-18 惠氏公司 Benzofurylalkanamine derivatives and their use as 5-HT2C agonists
US8242131B2 (en) * 2005-05-25 2012-08-14 Transcept Pharmaceuticals, Inc. Methods of treating middle-of-the-night insomnia
US20070225322A1 (en) * 2005-05-25 2007-09-27 Transoral Pharmaceuticals, Inc. Compositions and methods for treating middle-of-the night insomnia
US20070287740A1 (en) * 2005-05-25 2007-12-13 Transcept Pharmaceuticals, Inc. Compositions and methods of treating middle-of-the night insomnia
WO2006126718A1 (en) * 2005-05-27 2006-11-30 Tanabe Seiyaku Co., Ltd. Pyrazolopyrimidine derivative
TW200800959A (en) 2005-06-10 2008-01-01 Wyeth Corp Piperazine-piperidine antagonists and agonists of the 5-HT1a receptor
CA2611979A1 (en) * 2005-06-15 2006-12-21 Pfizer Limited Substituted arylpyrazoles
AU2006283592A1 (en) 2005-08-22 2007-03-01 Amgen Inc. Pyrazolopyridine and pyrazolopyrimidine compounds useful as kinase enzymes modulators
RU2008135326A (en) * 2006-03-24 2010-04-27 Вайет (Us) THERAPEUTIC COMPOSITIONS FOR THE TREATMENT OF DEPRESSION
MX2008012928A (en) 2006-04-04 2009-03-06 Univ California P13 kinase antagonists.
EA200802118A1 (en) 2006-04-07 2009-04-28 Девелоджен Ациенгезельшафт HAVING INHIBITING ACTIVITY WITH RESPECT TO MNK1 / MNK2 THYENOPYRIMIDINES INTENDED FOR USE IN PHARMACEUTICAL COMPOSITIONS
DE102006029074A1 (en) 2006-06-22 2007-12-27 Friedrich-Schiller-Universität Jena 4-Amino-3-arylamino-6-arylpyrazolo [3,4-d] pyrimidine derivatives, process for their preparation and their use as antiviral agents
EP1889847A1 (en) 2006-07-10 2008-02-20 DeveloGen Aktiengesellschaft Pyrrolopyrimidines for pharmaceutical compositions
PL2529621T3 (en) * 2006-09-22 2017-06-30 Pharmacyclics Llc Inhibitors of bruton's tyrosine kinase
TW200901974A (en) 2007-01-16 2009-01-16 Wyeth Corp Compounds, compositions, and methods of making and using them
GB2467670B (en) 2007-10-04 2012-08-01 Intellikine Inc Chemical entities and therapeutic uses thereof
CA2706203A1 (en) * 2007-11-22 2009-05-28 Boehringer Ingelheim International Gmbh Use of mnk inhibitors for the treatment of alzheimer's disease
ES2647163T3 (en) 2008-01-04 2017-12-19 Intellikine, Inc. Purine-substituted isoquinolinone derivatives useful as PI3K inhibitors
US8193182B2 (en) 2008-01-04 2012-06-05 Intellikine, Inc. Substituted isoquinolin-1(2H)-ones, and methods of use thereof
RU2357966C1 (en) * 2008-02-12 2009-06-10 Федеральное государственное образовательное учреждение высшего профессионального образования Кубанский государственный аграрный университет N-SUBSTITUTED PYRAZOLO[3,4-b]PYRIDYL-3-SULPHONYLAMINES DEVELOPING GROWTH-REGULATING ACTIVITY
EP2254420A4 (en) 2008-02-20 2012-02-15 Targia Pharmaceuticals Cns pharmaceutical compositions and methods of use
EP2252293B1 (en) 2008-03-14 2018-06-27 Intellikine, LLC Kinase inhibitors and methods of use
US8993580B2 (en) 2008-03-14 2015-03-31 Intellikine Llc Benzothiazole kinase inhibitors and methods of use
WO2009128383A1 (en) 2008-04-15 2009-10-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 3-PHENYLPYRAZOLO[5,1-b]THIAZOLE COMPOUND
US8461389B2 (en) 2008-04-18 2013-06-11 University College Dublin, National University Of Ireland, Dublin Psycho-pharmaceuticals
US20110224223A1 (en) 2008-07-08 2011-09-15 The Regents Of The University Of California, A California Corporation MTOR Modulators and Uses Thereof
AU2009268611B2 (en) 2008-07-08 2015-04-09 Intellikine, Llc Kinase inhibitors and methods of use
CA2735361A1 (en) 2008-08-26 2010-03-04 Boehringer Ingelheim International Gmbh Thienopyrimidines for pharmaceutical compositions
JP5731978B2 (en) 2008-09-26 2015-06-10 インテリカイン， エルエルシー Heterocyclic kinase inhibitor
CA2740885C (en) * 2008-10-16 2018-04-03 The Regents Of The University Of California Fused ring heteroaryl kinase inhibitors
US8476431B2 (en) 2008-11-03 2013-07-02 Itellikine LLC Benzoxazole kinase inhibitors and methods of use
JP5789252B2 (en) 2009-05-07 2015-10-07 インテリカイン， エルエルシー Heterocyclic compounds and uses thereof
AR078521A1 (en) 2009-10-08 2011-11-16 Eisai R&D Man Co Ltd PIRAZOLOTIAZOL COMPOUND
WO2011047384A2 (en) 2009-10-16 2011-04-21 The Regents Of The University Of California Methods of inhibiting ire1
EA201201191A1 (en) 2010-02-26 2013-04-30 Бёрингер Ингельхайм Интернациональ Гмбх 4- [CYCLOALKYLOXY (HETERO) ARYLAMINO] THIENO [2,3-D] PYRIMIDINES THAT HAVE INHIBITING ACTIVITY WITH RESPECT TO MNKL / MNK2 INTENDED FOR PHARMACEUTICAL COMPOSITIONS
TW201141483A (en) 2010-02-26 2011-12-01 Boehringer Ingelheim Int Thienopyrimidines containing a substituted alkyl group for pharmaceutical compositions
UY33241A (en) 2010-02-26 2011-09-30 Boehringer Ingelheim Int ? Tienopyrimidines containing heterocycloalkyl for pharmaceutical compositions ?.
AR080711A1 (en) * 2010-03-31 2012-05-02 Lilly Co Eli PIPERAZIN-PURINA COMPOSITE PHARMACEUTICAL COMPOSITION THAT INCLUDES IT AND ITS USE TO PREPARE A USEFUL MEDICINAL PRODUCT FOR THE TREATMENT OR PREVENTION OF PAIN
US8604032B2 (en) 2010-05-21 2013-12-10 Infinity Pharmaceuticals, Inc. Chemical compounds, compositions and methods for kinase modulation
EA201390421A1 (en) 2010-09-22 2013-09-30 Арена Фармасьютикалз, Инк. GPR119 RECEPTOR MODULATORS AND TREATMENT OF RELATED DISORDERS
EP2637669A4 (en) 2010-11-10 2014-04-02 Infinity Pharmaceuticals Inc Heterocyclic compounds and uses thereof
KR20180080358A (en) 2011-01-10 2018-07-11 인피니티 파마슈티칼스, 인코포레이티드 Processes for preparing isoquinolinones and solid forms of isoquinolinones
CA2828483A1 (en) 2011-02-23 2012-11-01 Intellikine, Llc Combination of kinase inhibitors and uses thereof
US8969363B2 (en) 2011-07-19 2015-03-03 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
WO2013012918A1 (en) 2011-07-19 2013-01-24 Infinity Pharmaceuticals Inc. Heterocyclic compounds and uses thereof
WO2013023184A1 (en) * 2011-08-11 2013-02-14 Intellikine, Llc Kinase inhibitor polymorphs
CN103998442B (en) 2011-08-29 2016-09-14 无限药品股份有限公司 Heterocyclic compound and application thereof
WO2013077921A2 (en) 2011-09-02 2013-05-30 The Regents Of The University Of California Substituted pyrazolo[3,4-d]pyrimidines and uses thereof
JP6071012B2 (en) 2011-10-14 2017-02-01 ドリッテ パテントポルトフォーリオ ベタイリグングスゲゼルシャフト エムベーハー ウント コー．カーゲー 4-Amino-3-phenylamino-6-phenylpyrazolo [3,4-d] pyrimidine derivatives, their preparation and use as antiviral agents
DE102012004736A1 (en) 2011-10-20 2013-04-25 Dritte Patentportfolio Beteiligungsgesellschaft Mbh & Co.Kg New 4-amino-3-phenylamino-6-phenylpyrazolo(3,4-d)pyrimidine derivatives useful as a medicament for prophylactic- or therapeutic treatment of viral infections, preferably picornavirus infections and rhinovirus infections
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
US8828998B2 (en) 2012-06-25 2014-09-09 Infinity Pharmaceuticals, Inc. Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
WO2014052669A1 (en) 2012-09-26 2014-04-03 The Regents Of The University Of California Modulation of ire1
DK2914296T4 (en) 2012-11-01 2022-01-03 Infinity Pharmaceuticals Inc Treatment of cancers using PI3 kinase isoform modulators
JP6440625B2 (en) 2012-11-14 2018-12-19 ザ・ジョンズ・ホプキンス・ユニバーシティー Methods and compositions for treating schizophrenia
US9481667B2 (en) 2013-03-15 2016-11-01 Infinity Pharmaceuticals, Inc. Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
ES2900806T3 (en) 2013-10-04 2022-03-18 Infinity Pharmaceuticals Inc Heterocyclic compounds and uses thereof
WO2015051241A1 (en) 2013-10-04 2015-04-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
SG10201808053XA (en) 2014-03-19 2018-10-30 Infinity Pharmaceuticals Inc Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders
US20150320755A1 (en) 2014-04-16 2015-11-12 Infinity Pharmaceuticals, Inc. Combination therapies
WO2016054491A1 (en) 2014-10-03 2016-04-07 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
EP4445956A3 (en) 2015-01-06 2024-12-04 Arena Pharmaceuticals, Inc. Compound for use in treating conditions related to the s1p1 receptor
EP3064207B1 (en) * 2015-03-04 2017-12-20 Scandion Oncology A/S 4-amino-3-phenylamino-6-phenylpyrazolo[3,4-d]pyrimidine derivatives for use as BCRP inhibitors in therapeutic treatments
PL3310760T3 (en) 2015-06-22 2023-03-06 Arena Pharmaceuticals, Inc. Crystalline l-arginine salt of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclo-penta[b]indol-3-yl)acetic acid for use in s1p1 receptor-associated disorders
JP6980649B2 (en) 2015-09-14 2021-12-15 インフィニティー ファーマシューティカルズ， インコーポレイテッド The solid form of the isoquinolinone derivative, the method for producing it, the composition containing it, and the method for using it.
WO2017161116A1 (en) 2016-03-17 2017-09-21 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
WO2017214269A1 (en) 2016-06-08 2017-12-14 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CA3028718A1 (en) 2016-06-24 2017-12-28 Infinity Pharmaceuticals, Inc. Combination therapies
WO2018081451A1 (en) 2016-10-26 2018-05-03 Indiana University Research And Technology Corporation Small molecule protein arginine methyltransferase 5 (prmt5) inhibitors and methods of treatment
WO2019169113A1 (en) * 2018-03-02 2019-09-06 Ponce Medical School Foundation, Inc. Compositions and methods for the treatment of endometriosis
CA3102136A1 (en) 2018-06-06 2019-12-12 Arena Pharmaceuticals, Inc. Methods of treating conditions related to the s1p1 receptor
CN110734439A (en) * 2019-11-07 2020-01-31 中国药科大学 A kind of parent nucleus is pyrazolo[3,4-d]pyrimidine compound and preparation method thereof
CN115151550B (en) * 2019-12-23 2024-11-22 桑福德·伯纳姆·普雷比医学发现研究所 Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) regulators and their uses

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2965643A (en) 1960-12-20 Derivatives of pyrazolo
US3551428A (en) 1956-02-10 1970-12-29 Ciba Geigy Corp New 1- (or 2-) substituted 4-mercapto-pyrazolo(3,4-d)pyrimidines
CH367510A (en) 1957-11-27 1963-02-28 Ciba Geigy Process for the production of new sulfonamides
FR1311787A (en) * 1961-05-10 1962-12-14 Ciba Geigy Process for the preparation of 4-mercapto-pyrazolo [3, 4-d] pyrimidines
FR2073274A1 (en) * 1969-12-15 1971-10-01 Sapchim Fournier Cimag Sa 4-mercapto-pyrazolo(3,4-d)-pyrimidines prepn
DE2430454A1 (en) * 1974-06-25 1976-01-15 Thomae Gmbh Dr K 4,6-Bis (cyclic amino)-pyrazolo/3,4-d/pyrimidine derivs - prepd by e.g. reacting 4,6 -dihalo cpds with cyclic amines
US4138705A (en) * 1977-04-22 1979-02-06 Lockwood Corporation Over-power safety device for motor driven system
US4139705A (en) 1977-05-20 1979-02-13 The Dow Chemical Company Pyrazolopyrimidines
JPS58208283A (en) 1982-05-28 1983-12-03 Shigeji Ueda Preparation of solvent having no change with days using furfuryl alcohol as raw material
US4426384A (en) 1982-08-05 1984-01-17 John R. A. Simoons Treatment of rheumatoid arthritis and related diseases
IT1154024B (en) 1982-09-22 1987-01-21 Lepetit Spa PRIDINICAL DERIVATIVES AND PROCEDURE FOR THEIR PRODUCTION
US4605642A (en) 1984-02-23 1986-08-12 The Salk Institute For Biological Studies CRF antagonists
DE3712735A1 (en) * 1987-04-15 1988-11-10 Boehringer Mannheim Gmbh NEW PYRAZOLO (3,4-D) PYRIMIDINE, METHOD FOR THE PRODUCTION AND USE THEREOF AS A MEDICINAL PRODUCT
US5153352A (en) 1988-10-25 1992-10-06 Bristol-Myers Squibb Company Process for preparation of intermediates of carbocyclic nucleoside analogs
US5391739A (en) * 1989-03-29 1995-02-21 Merrell Dow Pharmaceuticals Inc. Selective adenosine receptor agents
US5063245A (en) * 1990-03-28 1991-11-05 Nova Pharmaceutical Corporation Corticotropin-releasing factor antagonism compounds
FI933303A7 (en) 1991-01-23 1993-08-31 Gensia Inc Adenosine kinase inhibitors
AU665184B2 (en) * 1991-01-23 1995-12-21 Gensia, Inc. Adenosine kinase inhibitors
TW444018B (en) * 1992-12-17 2001-07-01 Pfizer Pyrazolopyrimidines
US5646152A (en) * 1994-06-15 1997-07-08 Pfizer Inc. Methods of administering CRF antagonists
US5593997A (en) * 1995-05-23 1997-01-14 Pfizer Inc. 4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors

Also Published As

Publication number Publication date
MY115300A (en) 2003-05-31
EP0674642A1 (en) 1995-10-04
FI935675A0 (en) 1993-12-16
CA2150709A1 (en) 1994-06-23
CA2150709C (en) 1999-03-16
NZ259114A (en) 1997-03-24
FI105920B (en) 2000-10-31
CZ158695A3 (en) 1995-11-15
AU5728194A (en) 1994-07-04
ES2150482T3 (en) 2000-12-01
GR3034507T3 (en) 2000-12-29
EG20273A (en) 1998-05-31
KR0167395B1 (en) 1999-01-15
TW370529B (en) 1999-09-21
AU680226B2 (en) 1997-07-24
DE69329296T2 (en) 2000-12-28
NO952399L (en) 1995-08-16
JP2862375B2 (en) 1999-03-03
PL309359A1 (en) 1995-10-02
US6218397B1 (en) 2001-04-17
KR950704319A (en) 1995-11-17
IL107944A0 (en) 1994-04-12
NO952399D0 (en) 1995-06-16
HU9303613D0 (en) 1994-04-28
PT674642E (en) 2001-01-31
EP0674642B1 (en) 2000-08-23
CN1034175C (en) 1997-03-05
KR100225720B1 (en) 1999-10-15
FI935675L (en) 1994-06-18
HU221507B (en) 2002-10-28
ZA939405B (en) 1995-06-15
TW444018B (en) 2001-07-01
DE69329296D1 (en) 2000-09-28
RU2124016C1 (en) 1998-12-27
JPH07509728A (en) 1995-10-26
WO1994013677A1 (en) 1994-06-23
CN1094048A (en) 1994-10-26
IL107944A (en) 2000-12-06
PL177028B1 (en) 1999-09-30
ATE195738T1 (en) 2000-09-15
NO305437B1 (en) 1999-05-31
HUT70426A (en) 1995-10-30
CZ287319B6 (en) 2000-10-11
DK0674642T3 (en) 2000-09-18

Similar Documents

Publication Publication Date Title
BR9307648A (en) Pyrazolopyrimidines as crf antagonists
NO950297D0 (en) Prolinamidderivater
NO2006018I1 (en) Entekavir: (2-amino-1,9-dihydro-9α (1S, 3R, 4S) -4hydroxy-3- (hydroxymethyl) -2-methylenecyclopentylÜ-6H-purin-6-one and hydrates thereof, especially monohydrate
NO980313L (en) N- (aroyl) glycine-hydroxamic acid derivatives and related compounds
ES2122076T3 (en) DERIVATIVES OF NOR-BILIAR ACIDS, PROCEDURE FOR THE PREPARATION AND USE OF THESE COMPOUNDS AS MEDICINES.
MX9800483A (en) Piperazine derivatives and their use as 5-ht1a antagonists.
DK102892D0 (en) PURIN DERIVATIVES, PHARMACEUTICAL PREPARATIONS COMPREHENSIVE, AND INTERNAL USE RELATIONS
GR3003232T3 (en) Quinazoline derivative, processes for its production, and cerebral dysfunction remedying agent comprising it as active ingredient
ATE114154T1 (en) THIENOTRIAZOLODIAZEPINS AND THEIR PHARMACEUTICAL USE.
ZA858659B (en) Use of spergualin derivatives for the preparation of medicaments having immunosuppressive activity
DE69106425D1 (en) Sulfonylamine substituted bicyclic hydroxanoic acid derivatives.
DK0855398T3 (en) Sesquiterpene derivatives with antiviral activity
IL84096A0 (en) Therapeutic agent for the treatment of peptic ulcer disease comprising a purine derivative
MX9205408A (en) METHOD FOR TREATING HYPERTENSION.
FI941850A0 (en) A new compound, leustroducsin H, its preparation and therapeutic use
ITMI921151A1 (en) THERAPEUTICLY ACTIVE COMPOUNDS, PARTICULARLY WITH NOOTROPIC ACTIVITY AND PROCEDURE FOR THEIR PREPARATION

Legal Events

Date Code Title Description
EG Technical examination (opinion): publication of technical examination (opinion)
FC Decision: refusal
CKFC Appeal: appeal against refusal